Method for producing orthocarbonic acid trialkyl esters

ABSTRACT

A process is provided for the preparation of trialkyl orthocarboxylates by the electrochemical oxidation of alpha, beta-diketones or alpha, beta-hydroxyketones, the keto group being present in the form of a ketal group derived from C 1 - to C 4 -alkylalcohols and the hydroxyl group optionally being present in the form of an ether group derived from C 1 - to C 4 -alkylalcohols (ketals K), in the presence of C 1 - to C 4 -alcohols (alcohols A), the molar ratio of the ketals K to the alcohols A in the electrolyte being 0.2:1 to 10:1.

DESCRIPTION

[0001] The invention relates to a process for the preparation of trialkyl orthocarboxylates (orthoesters O) by the electrochemical oxidation of alpha, beta-diketones or alpha, beta-hydroxyketones, the keto group being present in the form of a ketal group derived from C₁- to C₄-alkylalcohols and the hydroxyl group optionally being present in the form of an ether group derived from C₁- to C₄-alkylalcohols (ketals K) ; in the presence of C₁- to C₄-alcohols (alcohols A), the molar ratio of the sum of the orthoesters (O) and the ketals (K) to the alcohols (A) in the electrolyte being 0.2:1 to 5:1.

[0002] DE-A-3606472, for example, discloses non-electrochemical processes for the preparation of trialkyl orthocarboxylates such as trimethyl orthoformate (TMOF), chloroform being reacted with sodium methylate.

[0003] J. Org. Chem., 20 (1955) 1573, further discloses the preparation of TMOF from hydrocyanic acid and methanol.

[0004] J. Amer. Chem. Soc., (1975) 2546, J. Org. Chem., 61 (1996) 3256, and Electrochim. Acta, 42 (1997) 1933, disclose electrochemical processes by which C—C single bonds between C atoms each carrying an alkoxy group can be oxidatively cleaved, but the specific formation of orthoester groups is not described.

[0005] Russ. Chem. Bull., 48 (1999) 2093, discloses that vicinal diketones present in the form of their acetals are decomposed to the corresponding dimethyl dicarboxylates by anodic oxidation using high charge quantities and in the presence of a large excess of methanol (cf. p. 2097, column 1, paragraph 5).

[0006] Canadian Journal of Chemistry, 50 (1972) 3424, describes the anodic oxidation of benzil tetramethyldiketal to trimethyl orthobenzoate in a more than 100-fold excess of methanol. According to the authors, however, the product yield is only 62% and the current efficiency 5%.

[0007] Journ. Am. Chem. Soc., (1963) 2525, describes the electrochemical oxidation of orthoquinone tetramethylketal to the corresponding orthoester in a basic methanol solution. The reaction was carried out in a basic methanol solution with a substrate concentration of 10%. The product yield was 77% with a current efficiency of 6% (16 F/mol). It has not been possible hitherto to prepare purely aliphatic orthoesters electrochemically.

[0008] It is an object of the present invention to provide an electrochemical process for the preparation of trialkyl orthocarboxylates in an economic manner and especially with a high current efficiency, high product yields and a high selectivity.

[0009] We have found that this object is achieved by the process described at the outset.

[0010] The process according to the invention is particularly suitable for the preparation of orthoesters I of general formula I:

[0011] in which the radicals are defined as follows:

[0012] R¹ is hydrogen, C₁- to C₂₀-alkyl, C₂- to C₂₀-alkenyl, C₂- to C₂₀-alkynyl, C₃- to C₁₂-cycloalkyl, C₄- to C₂₀-cycloalkylalkyl, C₄- to C₁₀-aryl or optionally monosubstituted to trisubstituted by C₁- to C₈-alkoxy or C₁- to C₈-alkoxycarbonyl;

[0013] R², R³ are C₁- to C₂₀-alkyl, C₃- to C₁₂-cycloalkyl or C₄- to C₂₀-cycloalkylalkyl, or R² and R³ together form C₂- to C₁₀-alkylene; and

[0014] R⁴ is C₁- to C₄-alkyl.

[0015] Said orthoesters are prepared starting from ketals II of general formula II:

[0016] in which the radicals are defined as follows:

[0017] R⁵ and R¹⁰ are as defined for R¹;

[0018] R⁶ and R⁷ are as defined for R²;

[0019] R⁸ is hydrogen if R⁹ is as defined for R¹, or is as defined for R²; and

[0020] R⁹ is as defined for R¹ or is —O—R².

[0021] It is also possible to obtain the orthoesters I in the form of a mixture with ketals IV of general formula IV:

[0022] in which the radicals are defined as follows:

[0023] R¹¹ is as defined for R⁴;

[0024] R¹² is as defined for R²; and

[0025] R¹³ and R¹⁴ are as defined for R¹.

[0026] Said orthoesters are prepared starting from ketals II in which R⁹ is exclusively as defined for R¹.

[0027] The process according to the invention can be used to particular advantage to prepare orthoesters of general formula Ia (orthoesters Ia):

[0028] in which the radicals are defined as follows:

[0029] R¹⁵ and R¹⁶ are as defined for R²;

[0030] R¹⁸ is as defined for R²;

[0031] R¹⁷ and R²⁰ are as defined for R⁴;

[0032] R¹⁹ is as defined for R²; and

[0033] X is C₂- to C₁₂-alkylene (orthoesters Ia)

[0034] Said orthoesters are prepared starting from ketals of general formula IIa:

[0035] in which the radicals are defined as follows:

[0036] R²¹ and R²² are as defined for R²;

[0037] R²³ is as defined for R⁸;

[0038] R²⁴ is as defined for R⁹; and

[0039] Y is as defined for X (ketals IIa).

[0040] The ketals used according to the invention are obtainable by generally known preparative. processes. In the case of ketals with functional groups, these are most easily prepared by starting from a precursor which carries a C—C double bond in place of the desired functional group, and then functionalizing said double bond by standard methods (cf. Synthesis, (1981) 501-522).

[0041] The process according to the invention can also be used to particular advantage to prepare orthoesters Ib, being compounds in which:

[0042] R¹ is hydrogen, C₁-C₂₀-alkyl, C₃-C₁₂-cycloalkyl or C₄-C₂₀-cycloalkylalkyl;

[0043] R², R³ are C₁- to C₂₀-alkyl, C₃- to C₁₂-cycloalkyl or C₄- to C₂₀-cycloalkylalkyl, or R² and R³ together form C₂- to C₁₀-alkylene; and

[0044] R⁴ is C₁- to C₄-alkyl (orthoesters Ib),

[0045] starting from ketals II in which the radicals are defined as follows:

[0046] R⁵ and R¹⁰ are as defined for R¹ in orthoesters Ib; and

[0047] R⁶ to R⁹ are as defined for R² or R³ in orthoesters Ib (ketals IIb).

[0048] Within the group of orthoesters Ib, the process according to the invention can be used especially to prepare orthoesters Ic, in which:

[0049] R¹ is hydrogen or C₁- to C₆-alkyl; and

[0050] R², R³ and R⁴ are methyl or ethyl (orthoesters Ic),

[0051] starting from ketals II in which the radicals are defined as follows:

[0052] R⁵ and R¹⁰ are as defined for R¹ in orthoesters Ic; and

[0053] R⁶ to R⁹ are as defined for R² or R³ in orthoesters Ic (ketals IIc).

[0054] In the ketals IIb and IIc the radicals R⁵ and R¹⁰ preferably have the same definition.

[0055] The process according to the invention can be used to very particular advantage to prepare methyl orthoformate (TMOF) or ethyl orthoformate or methyl or ethyl orthoacetate (orthoesters Id), the corresponding starting compounds being 1,1,2,2-tetramethoxyethane (TME) or 1,1,2,2-tetraethoxyethane (ketals IId).

[0056] In the electrolyte the molar ratio of the sum of the orthoesters (O) and the ketals K to the alcohols A is 0.2:1 to 5:1, preferably 0.2:1-2:1 and particularly preferably 0.3:1 to 1:1.

[0057] The conducting salts present in the electrolysis solution are generally alkali metal, tetra(C₁- to C₆-alkyl)ammonium or tri(C₁- to C₆-alkyl)benzylammonium salts. Suitable counterions are sulfate, hydrogensulfate, alkylsulfates, arylsulfates, halides, phosphates, carbonates, alkylphosphates, alkylcarbonates, nitrate, alcoholates, tetrafluoroborate or perchlorate.

[0058] The acids derived from the abovementioned anions are also suitable as conducting salts.

[0059] Methyltributylammonium methylsulfates (MTBS), methyltriethylammonium methylsulfate or methyltripropylmethylammonium methylsulfates are preferred.

[0060] Conventional cosolvents are optionally added to the electrolysis solution. These are the inert solvents with a high oxidation protential which are generally conventional in organic chemistry. Dimethyl carbonate or propylene carbonate may be mentioned as examples.

[0061] The process according to the invention can be carried out in any of the conventional types of electrolysis cell. It is preferably carried out continuously with non-compartmentalized flow-through cells.

[0062] When the process is carried out continuously, the feed rate of the educts is generally chosen so that the weight ratio of the ketals K used to the orthoesters I formed in the electrolyte is 10:1 to 0.05:1.

[0063] The current densities used to carry out the process are generally 1 to 1000 and preferably 10 to 100 mA/cm². The temperatures are conventionally −20 to 60° C. and preferably 0 to 60° C. The working pressure is generally atmospheric pressure. Higher pressures are preferably applied when the process is to be carried out at higher temperatures, in order to prevent the starting compounds or cosolvents from boiling.

[0064] Examples of suitable anode materials are noble metals such as platinum, or metal oxides such as ruthenium or chromium oxide or mixed oxides of the type RuO_(x)TiO_(x). Graphite or carbon electrodes are preferred.

[0065] Examples of suitable cathode materials are iron, steel, stainless steel, nickel, noble metals such as platinum, and graphite or carbon materials. Preferred systems have graphite as the anode and cathode or graphite as the anode and nickel, stainless steel or steel as the cathode.

[0066] When the reaction has ended, the electrolysis solution is worked up by general methods of separation. This is generally done by first distilling the electrolysis solution to give the individual compounds separately in the form of different fractions. These can be purified further, for example by crystallization, distillation or chromatography.

EXPERIMENTAL SECTION EXAMPLE 1

[0067] A non-compartmentalized cell with graphite electrodes in a bipolar arrangement was used. The total electrode surface area was 0.145 m² (anode and cathode). The electrolyte used was a solution consisting of 2 mol of methanol to 1 mol of TME and containing 2% by weight of MTBS as the conducting salt. Electrolysis was carried out at 300 A/m² and a charge quantity of 2 F, based on TME, was passed through the cell. The electrolysis temperature was 20° C. When the electrolysis had ended, the products were determined quantitatively by gas chromatography and qualitatively by GC coupled with MS. TMOF was formed with a selectivity of 77% for a TME conversion of 69%. The principal by-products were methyl formate and methylal.

EXAMPLE 2

[0068] 240.3 g of 1,1,2-trimethoxyethane, 320 g of methanol and 5.8 g of ammonium tetrafluoroborate were placed in an electrolysis cell 40 with an electrode surface area of 316.4 cm², but otherwise as described in Example 1, and subjected to electrolysis. The electrolysis conditions were as described in Example 1. The electrolysis products contained 9.5 GC area % of formaldehyde dimethylacetal and 5.9 GC area % of trimethyl orthoformate.

EXAMPLE 3

[0069] 89 g of 2,2,3,3-tetramethoxybutene (80% pure, prepared from diacetyl and trimethyl orthoformate), 64 g of methanol and 1.7 g of ammonium tetrafluoroborate were reacted in an electrolysis cell with an electrode surface area of 298.8 cm², but otherwise as described in Example 1. The electrolysis conditions were as described in Example 1. The electrolysis products contained 1.7 GC area % of trimethyl orthoacetate for a current quantity of 2 Faraday and 18 GC area % for a current quantity of 8 F.

EXAMPLE 4

[0070] In an electrolysis operated continuously at a current density of 310 A/m² on graphite electrodes with a methanol-to-1,1,2,2-tetramethoxyethane feed of 1.5 mol to 1 mol and an MTBS content of 8% by weight, the electrolysis products contained TMOF with a selectivity of 95% and a current efficiency of 78% for a TME conversion of 41%. 

We claim:
 1. A process for the preparation of trialkyl orthocarboxylates (orthoesters O) by the electrochemical oxidation of alpha, beta-diketones or alpha, beta-hydroxyketones, the keto group being present in the form of a ketal group derived from C₁- to C₄-alkylalcohols and the hydroxyl group optionally being present in the form of an ether group derived from C₁- to C₄-alkylalcohols (ketals K), in the presence of C₁- to C₄-alcohols (alcohols A), the molar ratio of the sum of the orthoesters (O) and the ketals K to the alcohols A in the electrolyte being 0.2:1 to 5:1.
 2. A process as claimed in claim 1 wherein the orthoesters I are compounds of general formula I:

in which the radicals are defined as follows: R¹ is hydrogen, C₁- to C₂₀-alkyl, C₂- to C₂₀-alkenyl, C₂- to C₂₀-alkynyl, C₃- to C₁₂-cycloalkyl, C₄- to C₂₀-cycloalkylalkyl, C₄- to C₁₀-aryl or optionally monosubstituted to trisubstituted by C₁- to C₈-alkoxy or C₁- to C₈-alkoxycarbonyl; R² and R³ are C₁- to C₂₀-alkyl, C₃- to C₁₂-cycloalkyl or C₄- to C₂₀-cycloalkylalkyl, or R² and R³ together form C₂- to C₁₀-alkylene; and R⁴ is C₁- to C₄-alkyl, starting from ketals II of general formula II:

in which the radicals are defined as follows: R⁵ and R¹⁰ are as defined for R¹; R⁶ and R⁷ are as defined for R²; R⁸ is hydrogen if R⁹ is as defined for R¹, or is as defined for R²; and R⁹ is as defined for R¹ or is —O—R².
 3. A process as claimed in claim 2 wherein the orthoesters I of general formula I are formed as a mixture with ketals IV of general formula IV:

in which the radicals are defined as follows: R¹¹ is as defined for R⁴; R¹² is as defined for R²; and R¹³ and R¹⁴ are as defined for R¹, starting from ketals II in which R⁹ is exclusively as defined for R¹.
 4. A process as claimed in claim 1 wherein the orthoesters I are compounds of general formula Ia:

in which the radicals are defined as follows: R¹⁵ and R¹⁶ are as defined for R²; R¹⁸ is as defined for R²; R¹⁷ and R²⁰ are as defined for R⁴; R¹⁹ is as defined for R²; and X is C₂- to C₁₂-alkylene (orthoesters Ia), starting from ketals of general formula IIa:

in which the radicals are defined as follows: R²¹ and R²² are as defined for R²; R²³ is as defined for R⁸; R²⁴ is as defined for R⁹; and Y is as defined for X (ketals IIa).
 5. A process as claimed in claim 2 wherein the orthoesters I are compounds in which: R¹ is hydrogen or C₁ to C₆alkyl; and R², R³ and R⁴ are methyl or ethyl (orthoesters Ic) starting from ketals II in which the radicals are defined as follows: R⁵ and R¹⁰ are as defined for R¹ in orthoesters Ic; and R⁶ to R⁹ are as defined for R² or R¹ in orthoesters Ic (ketals IIc).
 6. A process as claimed in claim 5 wherein the orthoesters I are methyl or ethyl orthoformate or methyl or ethyl orthoacetate (orthoesters Id), starting from 1,1,2,2-tetramethoxyethane or 1,1,2,2-tetraethoxyethane (ketals IId), or 1,1,2,2-tetramethoxypropane or 1,1,2,2-tetraethoxypropane, or 2,2,3,3-tetramethoxybutane or 2,2,3,3-tetraethoxybutane.
 7. A process as claimed in any of claims 1 to 6 which is carried out in an electrolyte containing tetra(C₁- to C₆-alkyl)ammonium or tri(C₁- to C₆-alkyl)benzylammonium salts as conducting salts with sulfate, hydrogensulfate, alkylsulfates, arylsulfates, halides, phosphates, carbonates, alkylphosphates, alkylcarbonates, nitrate, alcoholates, tetrafluoroborate or perchlorate as counterions.
 8. A process as claimed in any of claims 1 to 7 wherein the conducting salt used is methyltributylammonium ethylsulfate, methyltripropylammonium methylsulfate, methyltriethylammonium methylsulfate or tetramethylammonium methylsulfate.
 9. A process as claimed in any of claims 1 to 8 which is carried out in a non-compartmentalized electrolysis cell.
 10. A process as claimed in any of claims 1 to 9 wherein the charge quantity per mol of converted alpha,beta-diketone or alpha,beta-hydroxyketone is 2 to 4 F. 